Composition for window film, flexible window film formed therefrom, and flexible display device comprising same

ABSTRACT

Provided are: a composition for a window film; a flexible window film formed therefrom; and a flexible display device comprising the same, wherein the composition contains: a siloxane resin comprising chemical Chemical Formula 1 or 2 or a mixture thereof; a cross-linking agent; and an initiator, the cross-linking agent being contained in a content of about 10-30 parts by weight on the basis of 100 parts by weight of the siloxane resin or the mixture thereof.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a National Phase Patent Application and claims priority to and the benefit of International Application Number PCT/KR2015/013827, filed on Dec. 16, 2015, which claims priority to and the benefit of Korean Application No. 10-2014-0182744, filed on Dec. 17, 2014, the entire contents of each of which are incorporated herein by reference.

BACKGROUND 1. Field

The present invention relates to a composition for window films, a flexible window film produced therefrom, and a flexible display comprising the same.

2. Description of the Related Art

Recently, a flexible display capable of being folded or unfolded has been developed in the related art. The flexible display is thin and light, has high impact resistance, can be folded and unfolded, and thus can be manufactured in various shapes.

In such a flexible display, not only a substrate but also various elements are required to have flexibility. Particularly, since a window film is disposed at the outermost side of the display, it is necessary for the window film to have flexibility, high hardness and optical reliability. Further, since the window film is manufactured by coating and curing a composition for window films on a base layer, the window film can suffer from curling.

SUMMARY

It is one aspect of the present invention to provide a composition for window films, which can realize a flexible window film capable of suppressing curling.

It is another aspect of the present invention to provide a composition for window films, which can realize a flexible window film having good properties in terms of hardness, flexibility and optical reliability such as light resistant reliability.

It is a further aspect of the present invention to provide a flexible window film, which can suppress curling and has good properties in terms of hardness, flexibility and optical reliability such as light resistant reliability, and a flexible display including the same.

In accordance with one aspect of the present invention, a composition for window films includes: a siloxane resin represented by Chemical Formula 1 or a siloxane resin represented by Chemical Formula 2 or a mixture thereof; a crosslinking agent; and an initiator, the crosslinking agent is present in an amount of about 10 parts by weight to about 30 parts by weight relative to 100 parts by weight of the siloxane resin or the mixture thereof: (R¹SiO_(3/2))_(x)(R²SiO_(3/2))_(y)  <Chemical Formula 1> (wherein Chemical Formula 1, R₁ and R₂ are the same as defined in the following detailed description; and 0<x≤1, 0≤y<1, and x+y=1), (R¹SiO_(3/2))_(x)(R³R⁴SiO_(2/2))_(z)(R²SiO_(3/2))_(y)  <Chemical Formula 2> (wherein Chemical Formula 2, R¹, R², R³ and R⁴ are the same as defined in the following detailed description; and 0<x<1, 0<y<1, 0<z<1, and x+y+z=1).

In accordance with another aspect of the present invention, a flexible window film includes: a base layer and a coating layer formed on one surface of the base layer, wherein the flexible window film has a curling of about 1.0 mm or less and the coating layer is formed of the composition for window films as set forth above.

In accordance with a further aspect of the present invention, a flexible display includes the flexible window film as set forth above.

The present invention provides a composition for window films, which can realize a flexible window film capable of suppressing curling.

The present invention provides a composition for window films, which can realize a flexible window film having good properties in terms of hardness, flexibility and optical reliability such as light resistant reliability.

The present invention provides a flexible window film, which can suppress curling and has good properties in terms of hardness, flexibility and optical reliability such as light resistant reliability, and a flexible display including the same.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a cross-sectional view of a flexible window film according to one embodiment of the present invention.

FIG. 2 is a cross-sectional view of a flexible window film according to another embodiment of the present invention.

FIG. 3 is a cross-sectional view of a flexible display according to one embodiment of the present invention.

FIG. 4 is a cross-sectional view of one embodiment of a display part shown in FIG. 3.

FIG. 5 is a cross-sectional view of a flexible display according to another embodiment of the present invention.

FIG. 6 is a cross-sectional view of a flexible display according to a further embodiment of the present invention.

FIG. 7 is a diagram illustrating a method of measuring a curling.

DETAILED DESCRIPTION

Embodiments of the present invention will be described in detail with reference to the accompanying drawings. It should be understood that the present invention is not limited to the following embodiments and may be embodied in different ways. In the drawings, portions irrelevant to the description will be omitted for clarity. Like components will be denoted by like reference numerals throughout the specification.

Herein, spatially relative terms such as “upper” and “lower” are defined with reference to the accompanying drawings. Thus, it will be understood that the term “upper surface” can be used interchangeably with the term “lower surface”. In addition, when an element such as a layer or a film is referred to as being placed “on” another element, it can be directly placed on the other element, or intervening element(s) may be present. On the other hand, when an element is referred to as being placed “directly on” another element, there are no intervening element(s) therebetween.

Herein, the term “pencil hardness” is measured on a coating layer of a window film using a pencil hardness tester (Heidon) in accordance with JIS K5400. In measurement of pencil hardness, pencils of 6B to 9H (Mitsubishi Co., Ltd.) are used. Specifically, pencil hardness is measured under conditions of a pencil load of 1 kg on the coating layer, a scratch angle of 45°, and a scratch speed of 60 mm/m in. When the coating layer has one or more scratches after being tested 5 times using a certain pencil, pencil hardness is measured again using another pencil having one-level lower pencil hardness than the previous pencil, and the maximum value of pencil hardness allowing no scratch to be observed all five times on the coating layer is taken as pencil hardness of the coating layer.

Herein, the term “radius of curvature” refers to a minimum radius of a jig causing no cracks on a window film specimen when the window film specimen is wound around the jig for measuring a radius of curvature (CFT-200R, COVOTECH Co., Ltd.), kept wound for 5 seconds, unwound, and then observed with the naked eye to determine whether the specimen has cracks. Here, a radius of curvature in a compressive direction is measured when the specimen is wound around the jig such that a window coating layer of the window film contacts a surface of the jig, and a radius of curvature in a tensile direction is measured when the specimen is wound around the jig such that a base layer of the window film contacts the jig. Here, the window film specimen has a thickness of 50 μm to 300 μm.

Herein, the term “ΔY.I.” refers to a difference (Y2−Y1) between a yellow index (Y1) measured on a window film under a D65 light source at 2° (angle between the window film and the light source) using a colorimeter (CM3600D, Konica Minolta) and a yellow index (Y2) measured on the window film by the same method after irradiating the window film at a peak wavelength of 306 nm for 72 hours using a light resistance tester (CT-UVT, Core Technology Inc.).

Herein, referring to FIG. 7, the term “curl” means average value of a maximum height (H) from a floor (2) to a window film (1) placed on the floor (2) such that a base layer of the window film (2) contacts the floor, as measured after the window film (1) is left under conditions of 22° C. to 28° C. and 30% relative humidity to 50% relative humidity.

Herein, the term “(meth)acryl” refers to acryl and/or methacryl. Herein, unless otherwise stated, “substituted” means that at least one hydrogen atom in a functional group is substituted with a hydroxyl group, an unsubstituted C₁ to C₁₀ alkyl group, a C₁ to C₁₀ alkoxy group, a C₃ to C₁₀ cycloalkyl group, a C₆ to C₂₀ aryl group, a C₇ to C₂₀ arylalkyl group, a benzophenone group, a C₆ to C₂₀ aryl group substituted with a C₁ to C₁₀ alkyl group, or a C₁ to C₁₀ alkyl group substituted with a C₁ to C₁₀ alkoxy group.

Herein, the term “crosslinkable functional group” means a functional group allowing crosslinking reaction by heat and/or light. For example, the crosslinkable functional group means an epoxy group, an epoxy group-containing group, a glycidyl group, a glycidyl group-containing group, a glycidoxy group, a glycidoxy group-containing group, an oxetanyl group, an oxetanyl group-containing group, and the like. Specifically, the crosslinkable functional group means an epoxy group; a glycidyl group; a glycidoxy group; an oxetanyl group; an oxetanyloxy group; an epoxy group, a glycidyl group, a glycidoxy group, an epoxylated C₅ to C₂₀ cycloalkyl group, an epoxylated C₁ to C₁₀ alkyl group, an oxetanyl group or an oxetanyloxy group-containing C₁ to C₂₀ alkyl group; or an epoxy group, a glycidyl group, a glycidoxy group, an epoxylated C₅ to C₂₀ cycloalkyl group, an epoxylated C₁ to C₁₀ alkyl group, or an oxetanyl group or oxetanyloxy group-containing C₅ to C₂₀ cycloalkyl group, and may be unsubstituted or substituted with another element. Herein, the term “UV absorption functional group” means a functional group capable of absorbing light at a wavelength of about 400 nm or less, for example, about 100 nm to about 400 nm. Specifically, the UV absorption functional group may include an unsubstituted or substituted benzotriazole group, an unsubstituted or substituted benzophenone group, an unsubstituted or substituted hydroxybenzophenone group, an unsubstituted or substituted triazine group, an unsubstituted or substituted salicylate group, an unsubstituted or substituted cyanoacrylate group, an unsubstituted or substituted oxanilide group, an unsubstituted or substituted hydroxyphenyltriazine group, an unsubstituted or substituted hydroxyphenylbenzotriazole group, or an unsubstituted or substituted hydroxyphenylbenzophenone group, without being limited thereto.

Herein, the term “UV absorption functional group-containing group” means a group containing the UV absorption functional group. Herein, the term “alkyleneoxy group” means an alkylene group having oxygen (O) at a terminal or inner structure thereof. Herein, the term “halogen” means fluorine, chlorine, bromine, or iodine. Herein, “Ec” refers to a (3,4-epoxycyclohexyl)ethyl group, “Gp” refers to a 3-glycidoxypropyl group, “Op” refers to a 3-oxetanylpropyl group, and “Me” refers to a methyl group.

Hereinafter, a composition for window films according to one embodiment of the present invention will be described.

The composition for window films according to the embodiment includes: a siloxane resin comprising a compound represented by Chemical Formula 1 or Chemical Formula 2 or a mixture thereof, a crosslinking agent and an initiator, the crosslinking agent is present in an amount of about 10 parts by weight to about 30 parts by weight relative to 100 parts by weight of the siloxane resin or the mixture thereof: (R¹SiO_(3/2))_(x)(R²SiO_(3/2))_(y)  <Chemical Formula 1> (wherein Chemical Formula 1, R¹ is a crosslinkable functional group; R² is a UV absorption functional group or a UV absorption functional group-containing group; and 0<x≤1, 0≤y<1, and x+y=1), (R¹SiO_(3/2))_(x)(R³R⁴SiO_(2/2))_(z)(R²SiO_(3/2))_(y)  <Chemical Formula 2> (wherein Chemical Formula 2, R¹ is a crosslinkable functional group; R² is a UV absorption functional group or a UV absorption functional group-containing group; R³ and R⁴ are each independently hydrogen, a crosslinkable functional group, an unsubstituted or substituted C₁ to C₂₀ alkyl group, or an unsubstituted or substituted C₅ to C₂₀ cycloalkyl group, at least one of R³ and R⁴ being an unsubstituted or substituted C₁ to C₂₀ alkyl group; and 0<x<1, 0<y<1, 0<z<1, and x+y+z=1).

With the siloxane resin comprising the compound represented by Chemical Formula 1 or Chemical Formula 2 or the mixture thereof, the composition for window films according to the embodiment can improve hardness, flexibility and optical reliability, such as light resistant reliability, of a window film formed of the same. In addition, the siloxane resin is prepared through adjustment of the content of each silicon monomer, thereby allowing easy adjustment of hardness, flexibility and optical reliability, such as light resistant reliability, of the window film. Specifically, in one embodiment, in Chemical Formula 1, 0.20≤x≤0.999, 0.001≤y≤0.80, more specifically 0.20≤x≤0.99, 0.01≤y≤0.80, still more specifically 0.80≤x≤0.99, 0.01≤y≤0.20. In another embodiment, Chemical Formula 1 may be represented by (R^(1a)SiO_(3/2))_(x1)(R^(1b)SiO_(3/2))_(x2) (R^(1a) and R^(1b) are different crosslinkable functional groups, 0<x1<1, 0<x2<1, and x1+x2=1), specifically 0.70≤x1<1 and 0<x2≤0.30, specifically 0.80≤x1<1 and 0<x2≤0.20, more specifically 0.85≤x1≤0.99 and 0.01≤x2≤0.15. In Chemical Formula 2, 0.40≤x≤0.99, 0.001≤y≤0.20, 0.001≤z≤0.40, more specifically 0.80≤x≤0.98, 0.001≤y)≤0.10, and 0.005≤z≤0.10, still more specifically 0.80≤x≤0.98, 0.01≤y≤0.10, and 0.01≤z≤0.10. Within this range, the siloxane resin can improve hardness, flexibility and light resistant reliability of the window film.

In Chemical Formula 1, R¹ can provide crosslinkability to the composition for window films. Specifically, R¹ may be a (3,4-epoxycyclohexyl)methyl group, a (3,4-epoxycyclohexyl)ethyl group, a (3,4-epoxycyclohexyl)propyl group, a 3-glycidoxypropyl group, a 3-oxetanylmethyl group, a 3-oxetanylethyl group, a 3-oxetanylpropyl group, or a 3-oxetanyloxy group. R² can absorb UV light. Specifically, R² may be an unsubstituted or substituted hydroxybenzophenone group, an unsubstituted or substituted hydroxyphenyltriazine group, or a group represented by Chemical Formula 3. *—(R^(x))_(n1)-M-(R^(x))_(n2)—R^(y)  <Chemical Formula 3> (wherein Chemical Formula 3, * is a linking site with respect to Si; R^(x) is an unsubstituted or substituted C₁ to C₂₀ alkylene group, an unsubstituted or substituted C₁ to C₂₀ alkyleneoxy group, an unsubstituted or substituted C₁ to C₂₀ alkylene group having a urethane group at a terminal or inner structure thereof, an unsubstituted or substituted C₁ to C₂₀ alkyleneoxy group having a urethane group at a terminal or inner structure thereof, an unsubstituted or substituted C₆ to C₂₀ arylene group, or a combination thereof, n1 and n2 are each independently 0 or 1, M is a single bond, oxygen (O), sulfur (S), NR (R being hydrogen or a C₁ to C₁₀ alkyl group), —CONH—, —OCONH—, —C═O—, or —C═S—, and R^(y) is an unsubstituted or substituted benzotriazol group, an unsubstituted or substituted benzophenone group, an unsubstituted or substituted hydroxybenzophenone group, an unsubstituted or substituted triazine group, an unsubstituted or substituted salicylate group, an unsubstituted or substituted cyanoacrylate group, an unsubstituted or substituted oxanilide group, an unsubstituted or substituted hydroxyphenyltriazine group, an unsubstituted or substituted hydroxyphenylbenzotriazol group, or an unsubstituted or substituted hydroxyphenylbenzophenone group).

Specifically, R^(x) is an unsubstituted or substituted C₁ to C₂₀ alkylene group or an unsubstituted or substituted C₁ to C₂₀ alkyleneoxy group. M may be oxygen (O) or —OCONH—. R^(y) may be an unsubstituted or substituted hydroxybenzophenone group or an unsubstituted or substituted hydroxyphenyltriazine group. More specifically, R^(y) may be a 2-hydroxybenzophenone group, a 2,4-dihydroxybenzophenone group, a 2,2′-dihydroxybenzophenone group, a 2-hydroxy-4-methoxybenzophenone group, a 2-hydroxy-4-methoxy-4′-methylbenzophenone group, a 2,2′-dihydroxy-4-methoxybenzophenone group, a 2,4,4′-trihydroxybenzophenone group, a 2,2′,4,4′-tetrahydroxybenzophenone group, a 2,3,4,4′-tetrahydroxybenzophenone group, a 2,3′4,4′-tetrahydroxybenzophenone group, or a 2,2′-dihydroxy-4,4′-dimethoxybenzophenone group, or a group represented by Chemical Formula 3-1:

(wherein Chemical Formula 3-1, * is a linking site). R³ and R⁴ can provide crosslinkability and flexibility to the composition for window films. Specifically, R³ may be an unsubstituted or substituted C₁ to C₂₀ alkyl group and R₄ may be a crosslinkable functional group. R³ and R⁴ can further improve hardness of a window film by further improving crosslinkability of the composition for window films. More specifically, R³ and R⁴ are each independently a (3,4-epoxycyclohexyl)methyl group, a (3,4-epoxycyclohexyl)ethyl group, a (3,4-epoxycyclohexyl)propyl group, a glycidoxy propyl group, a methyl group, an ethyl group, an n-propyl group, or an isopropyl group.

Specifically, the siloxane resin comprising the compound represented by Chemical Formula 1 may include at least one of Chemical Formulae 1-1 to 1-13, without being limited thereto: (EcSiO_(3/2))_(x)(RaSiO_(3/2))_(y)  <Chemical Formula 1-1> (ECSiO_(3/2))_(x)(RbSiO_(3/2))_(y)  <Chemical Formula 1-2> (EcSiO_(3/2))_(x)(RcSiO_(3/2))_(y)  <Chemical Formula 1-3> (EcSiO_(3/2))_(x)(RdSiO_(3/2))_(y)  <Chemical Formula 1-4> (GpSiO_(3/2))_(x)(RaSiO_(3/2))_(y)  <Chemical Formula 1-5> (GpSiO_(3/2))_(x)(RbSiO_(3/2))_(y)  <Chemical Formula 1-6> (GpSiO_(3/2))_(x)(RcSiO_(3/2))_(y)  <Chemical Formula 1-7> (GpSiO_(3/2))_(x)(RdSiO_(3/2))_(y)  <Chemical Formula 1-8> (OpSiO_(3/2))_(x)(RaSiO_(3/2))_(y)  <Chemical Formula 1-9> (OpSiO_(3/2))_(x)(RbSiO_(3/2))_(y)  <Chemical Formula 1-10> (OpSiO_(3/2))_(x)(RcSiO_(3/2))_(y)  <Chemical Formula 1-11> (OpSiO_(3/2))_(x)(RdSiO_(3/2))_(y)  <Chemical Formula 1-12> (in Chemical Formulae 1-1 to 1-12, Ra is represented by Chemical Formula i); Rb is represented by Chemical Formula ii); Rc is represented by Chemical Formula iii); and Rd is represented by Chemical Formula iv),

(in Chemical Formulae i to iv, * is a linking site); and 0<x<1, 0<y<1, and x+y=1). (EcSiO_(3/2))_(x1)(GpSiO_(3/2))_(x2)  <Chemical Formula 1-13> (in Chemical Formula 1-13, 0<x1<1, 0<x2<1, and x1+x2=1).

Specifically, the siloxane resin comprising the compound represented by Chemical Formula 2 may include at least one of compounds represented by Chemical Formulae 2-1 to 2-36, without being limited thereto: (EcSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-1> (EcSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-2> (EcSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-3> (ECSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-4> (EcSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-5> (EcSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-6> (EcSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-7> (EcSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-8> (EcSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-9> (ECSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-10> (EcSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-11> (ECSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-12> (GpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-13> (GpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-14> (GpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-15> (GpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-16> (GpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-17> (GpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-18> (GpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-19> (GpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-20> (GpSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-21> (GpSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-22> (GpSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-23> (GpSiO3/2)x(GpMeSiO_(2/2))z(RdSiO_(3/2))y  <Chemical Formula 2-24> (OpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-25> (OpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-26> (OpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-27> (OpSiO_(3/2))_(x)(EcMeSiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-28> (OpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-29> (OpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-30> (OpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-31> (OpSiO_(3/2))_(x)((Me)₂SiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-32> (OpSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RaSiO_(3/2))_(y)  <Chemical Formula 2-33> (OpSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RbSiO_(3/2))_(y)  <Chemical Formula 2-34> (OpSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RcSiO_(3/2))_(y)  <Chemical Formula 2-35> (OpSiO_(3/2))_(x)(GpMeSiO_(2/2))_(z)(RdSiO_(3/2))_(y)  <Chemical Formula 2-36> (in Chemical Formulae 2-1 to 2-36, Ra is represented by the Chemical Formula i); Rb is represented by the Chemical Formula ii); Rc is represented by the Chemical Formula iii); Rd is represented by the Chemical Formula iv); and 0<x<1, 0<y<1, 0<z<1, and x+y+z=1).

The siloxane resin comprising the compound represented by Chemical Formula 1 or Chemical Formula 2 may have a weight average molecular weight of about 4,000 to about 100,000, specifically about 4,500 to about 10,000, more specifically about 5,000 to about 7,000. Within this range, the siloxane resin can be easily produced and can provide good properties in terms of hardness and flexibility. The siloxane resin comprising the compound represented by Chemical Formula 1 or Chemical Formula 2 may have a polydispersion index (PDI) of about 1.0 to 3.0, specifically about 1.5 to 2.5, and an epoxy equivalent weight of about 0.1 mol/100 g to about 1.0 mol/100 g, specifically about 0.3 mol/100 g to about 0.7 mol/100 g. Within these ranges, the siloxane resin can provide stable coating properties to the window film.

The crosslinking agent may contain a crosslinkable functional group to improve hardness of the window film. The crosslinking agent may be present in an amount of about 10 parts by weight to about 30 parts by weight relative to 100 parts by weight of the siloxane resin or the mixture thereof. Within this range, the composition can provide a window film that can suppress curling and exhibits good hardness and flexibility.

Specifically, the crosslinking agent may include a non-cyclic aliphatic epoxy monomer, a cyclic aliphatic epoxy monomer, an aromatic epoxy monomer, a hydrogenated aromatic epoxy monomer, and an oxetane monomer. These crosslinking agents may be used alone or as a mixture thereof.

When the crosslinking agent comprises an epoxy monomer, the crosslinking agent may have an epoxy equivalent weight of about 0.5 mol/100 g to about 1.0 mol/100 g. Within this range, the composition can improve flexibility and hardness of the coating layer. The crosslinking agent may have a weight average molecular weight of about 200 g/mol to about 400 g/mol. Within this range, the composition can improve flexibility and hardness of the coating layer.

The non-cyclic aliphatic epoxy monomer may include 1,4-butanediol diglycidyl ether, 1,6-hexanediol diglycidyl ether, neopentylglycol diglycidyl ether, trimethylolpropane triglycidyl ether, polyethylene glycol diglycidyl ether, glycerin triglycidyl ether, and polypropylene glycol diglycidyl ether; polyglycidyl ethers of polyetherpolyol obtained by adding one or more types of alkylene oxide to aliphatic polyhydric alcohols, such as ethylene glycol, propylene glycol, glycerin, and the like; diglycidyl esters of aliphatic long-chain dibasic acids; monoglycidyl ethers of higher aliphatic alcohol; glycidyl ethers of higher fatty acids; epoxylated soybean oil; epoxy stearic acid butyl; epoxy stearic acid octyl; epoxylated linseed oil; epoxylated polybutadiene, and the like.

The cyclic aliphatic epoxy monomer is a compound having at least one epoxy group in an alicyclic group, and may include alicyclic epoxy carboxylate or alicyclic epoxy (meth)acrylate. Specifically, the cyclic aliphatic epoxy monomer may include (3,4-epoxycyclohexyl)methyl-3′,4′-epoxycyclohexanecarboxylate, 3,4-epoxy-6-methylcyclohexylmethyl-3′,4′-epoxy-6′-methylcyclohexanecarboxylate, diglycidyl 1,2-cyclohexanedicarboxylate, bis(3,4-epoxycyclohexylmethyl)adipate, bis((3,4-epoxy-6-methylcyclohexyl)methyl)adipate, ε-caprolactone modified 3,4-epoxycyclohexylmethyl-3′,4′-epoxycyclohexanecarboxylate, 1,4-cyclohexanedimethanol bis(3,4-epoxycyclohexanecarboxylate), 3,4-epoxycyclohexylmethyl(meth)acrylate, epoxycyclohexyl-5,5-spiro-3,4-epoxy)cyclohexane-metha-dioxane, trimethylcaprolactone modified 3,4-epoxycyclohexylmethyl-3′,4′-epoxycyclohexanecarboxylate, β-methyl-δ-valerolactone modified 3,4-epoxycyclohexylmethyl-3′,4′-epoxycyclohexanecarboxylate, ethylene glycol di(3,4-epoxycyclohexylmethyl)ether, ethylene bis(3,4-epoxycyclohexanecarboxylate), 4-vinylcyclohexen dioxide, vinylcyclohexen monoxide, bis(3,4-epoxycyclohexylmethyl)malonate, bis(3,4-epoxycyclohexylmethyl)succinate, bis(3,4-epoxycyclohexylmethyl)glutarate, bis(3,4-epoxycyclohexylmethyl)pimelate, bis(3,4-epoxycyclohexylmethyl)azelate, bis(3,4-epoxycyclohexylmethyl)sebacate, and the like.

The aromatic epoxy monomer may include bisphenol type epoxy resins such as diglycidyl ether of bisphenol A, diglycidyl ether of bisphenol F, and diglycidyl ether of bisphenol S; novolac type epoxy resins such as a phenol novolac epoxy resin, a cresol novolac epoxy resin, and a hydroxybenzaldehyde phenol novolac epoxy resin; and polyfunctional epoxy resins such as glycidyl ether of tetrahydroxyphenyl methane, glycidyl ether of tetrahydroxybenzophenone, and epoxylated polyvinyl phenol.

The hydrogenated aromatic epoxy monomer means a monomer obtained by selective hydrogenation of an aromatic epoxy monomer in the presence of a catalyst under pressure. The aromatic epoxy monomer for the hydrogenated aromatic epoxy monomer may include the aromatic epoxy monomer described above.

The oxetane monomer may include at least one selected from among 3-methyloxetane, 2-methyloxetane, 2-ethylhexyloxetane, 3-oxetanol, 2-methyleneoxetane, 3,3-oxetanedimethanethiol, 4-(3-methyloxetan-3-yl)benzonitrile, N-(2,2-dimethylpropyl)-3-methyl-3-oxetanmethaneamine, N-(1,2-dimethylbutyl)-3-methyl-3-oxetanmethaneamine, (3-ethyloxetan-3-yl)methyl(meth)acrylate, 4-[(3-ethyloxetan-3-Amethoxy]butan-1-ol, 3-ethyl-3-hydroxymethyloxetane, xylenebisoxetane, and 3-[ethyl-3[[(3-ethyloxetane-3-yl]methoxy]methyl]oxetane, without being limited thereto.

The initiator can cure the siloxane resins and the crosslinking agent described above. The initiator may include at least one of a photocationic initiator and a photo-radical initiator. The initiators may be used alone or as a mixture thereof.

As the photocationic initiator, any typical photocationic initiator known to those skilled in the art may be used. Specifically, the photocationic initiator may include an onium salt containing a cation and an anion. Specifically, examples of the cation may include: diaryliodonium such as diphenyliodonium, 4-methoxydiphenyliodonium, bis(4-methylphenyl)iodonium, bis(4-tert-butylphenyl)iodonium, bis(dodecylphenyl)iodonium, and (4-methylphenyl)[(4-(2-methylpropyl)phenyl)iodonium]; triarylsulfonium such as triphenylsulfonium, diphenyl-4-thiophenylphenylsulfonium, and diphenyl-4-thiophenoxyphenylsulfonium; bis[4-(diphenylsulfonio)phenyl]sulfide, and the like. Specifically, examples of the anion may include hexafluorophosphate (PF₆ ⁻), tetrafluoroborate (BF₄ ⁻), hexafluoroantimonate (SbF₆ ⁻), hexafluoroarsenate (AsF₆ ⁻), hexachloroantimonate (SbCl₆ ⁻), and the like.

As the photo-radical initiator, any photo-radical initiator known to those skilled in the art may be used. Specifically, the photo-radical initiator may include at least one of thioxanthone based, phosphorus based, triazine based, acetophenone based, benzophenone based, benzoin based, and oxime based photo-radical initiator.

The initiator may be present in an amount of about 0.01 parts by weight to about 20 parts by weight, specifically about 1 part by weight to about 10 parts by weight, relative to 100 parts by weight of the siloxane resin or the mixture thereof. Within this range, the siloxane resin can be sufficiently cured without deterioration in transparency of the window film due to the remaining initiator.

The composition for window films according to this embodiment may further include nanoparticles. The nanoparticles can further improve hardness of the window film. The nanoparticles may include at least one of silica, aluminum oxide, zirconium oxide, and titanium oxide, without being limited thereto. The nanoparticles may also be subjected to surface treatment with a silicone compound for mixing with the siloxane resin. The nanoparticles are not limited to a particular shape or size. Specifically, the nanoparticles may include spherical, flake, or amorphous particles. The nanoparticles may have an average particle size of about 1 nm to about 200 nm, specifically about 10 nm to about 50 nm. Within this range, the nanoparticles can increase hardness of the window film without affecting surface roughness and transparency of the window film. The nanoparticles may be present in an amount of about 0.1 parts by weight to about 60 parts by weight, specifically about 10 parts by weight to about 50 parts by weight, relative to 100 parts by weight of the siloxane resins or the mixture thereof. Within this range, the nanoparticles can increase hardness of the window film without affecting surface roughness and transparency thereof.

The composition for window films according to this embodiment may further include additives. The additives can provide additional functions to the window film. The additives may be any additives commonly used for window films in the related art. Specifically, the additives may include at least one of a UV absorbent, a reaction inhibitor, an adhesion promoter, a thixotropic agent, a conductivity imparting agent, a color adjusting agent, a stabilizer, an antistatic agent, an antioxidant, and a leveling agent, without being limited thereto. The reaction inhibitor may include ethynylcyclohexane, the adhesion promoter may be an epoxy or alkoxysilyl group-containing silane compound, and the thixotropic agent may be fumed silica. The conductivity imparting agent may include metal powder such as silver powder, copper powder, aluminum powder, and the like, and the color adjusting agent may include pigments, dyes, and the like. The UV absorbent can improve light resistant reliability of the window film. The UV absorbent may be any typical absorbent known to those skilled in the art. Specifically, the UV absorbent may include at least one of triazine based, benzimidazole based, benzophenone based, benzotriazole based, and hydroxyphenyltriazine based UV absorbents, without being limited thereto. The additives may be present in an amount of about 0.01 parts by weight to about 5 parts by weight, specifically about 0.1 parts by weight to about 2.5 parts by weight, relative to 100 parts by weight of the siloxane resins or the mixture thereof. Within this range, the additives can improve hardness and flexibility of the window film while realizing effects thereof.

The composition for window films according to this embodiment may further include a solvent to improve coatability, wettability or processability. The solvent may include methylethylketone, methylisobutylketone, and propylene glycol monomethyletheracetate, without being limited thereto.

The composition for window films according to this embodiment may have a viscosity of about 50 cP to about 2,000 cP at 25° C. Within this range, the composition allows easy formation of the window film.

Next, a method of preparing the siloxane resin comprising the compound represented by Chemical Formula 1 will be described in detail.

The siloxane resin comprising the compound represented by Chemical Formula 1 may be prepared through hydrolysis and condensation of a first silicon monomer only or a monomer mixture including the first silicon monomer and a second silicon monomer. In one embodiment, the first silicon monomer may be present in an amount of about 20 mol % to about 99.9 mol %, specifically about 20 mol % to about 99 mol %, more specifically about 80 mol % to about 99 mol % in the monomer mixture. The second silicon monomer may be present in an amount of about 0.1 mol % to about 80 mol %, specifically about 1 mol % to about 80 mol %, more specifically about 1 mol % to about 20 mol % in the monomer mixture. In another embodiment, one of the first silicon monomers may be preset in an amount of about 70 mol % to less than about 100 mol %, about 80 mol % to less than about 100 mol %, about 85 mol % to about 99 mol %, and the other one of the first silicon monomers may be present in an amount of more than about 0 mol % to about 30 mol %, more than about 0 mol % to 20 mol %, or about 1 mol % to 15 mol %. Within these ranges, the first and second silicon monomers can improve hardness and light resistant reliability of the window film.

The first silicon monomer may include a silane compound represented by Chemical Formula 4 and the second silicon monomer may include a silane compound represented by Chemical Formula 5. These may be used alone or in combination thereof:

(wherein Chemical Formula 4, R¹ is the same as defined in Chemical Formula 1, and R⁵, R⁶ and R⁷ are each independently a halogen, a hydroxyl group or a C₁ to C₁₀ alkoxy group).

(wherein Chemical Formula 5, R² is the same as defined in Chemical Formula 1, and R⁸, R⁹ and R¹⁰ are each independently a halogen, a hydroxyl group or a C₁ to C₁₀ alkoxy group).

Specifically, the first silicon monomer may include at least one selected from 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-oxetanylmethyltrimethoxysilane, 3-oxetanylethyltrimethoxysilane, 3-oxetanylpropyltrimethoxysilane, and 3-oxetanyloxytrimethoxysilane, without being limited thereto.

In one embodiment, the second silicon monomer may be prepared through reaction of benzophenone having two or more hydroxyl groups with an alkoxysilane. Specifically, the benzophenone having two or more hydroxyl groups may be 2,2′-dihydroxybenzophenone, 2,4-dihydroxybenzophenone, 2,2′-dihydroxy-4-methoxybenzophenone, 2,2′-dihydroxy-4-methoxy-4′-methylbenzophenone, 2,2′-dihydroxy-4-methoxybenzophenone, 2,4,4′-trihydroxybenzophenone, 2,2′,4,4′-tetrahydroxybenzophenone, 2,3,4,4′-tetrahydroxybenzophenone, 2,3′4,4′-tetrahydroxybenzophenone, or 2,2′-dihydroxy-4,4′-dimethoxybenzophenone. The alkoxysilane may include an alkoxysilane compound having one to three C₁ to C₅ alkoxy groups. The benzophenone having two or more hydroxyl groups and the alkoxysilane may be reacted in a mole ratio of 1:1 to 1:1.5. A platinum catalyst may be used in order to improve reaction efficiency. In another embodiment, the second silicon monomer may be prepared by reacting a UV absorbent known to those skilled in the art with an alkoxysilane compound having a functional group capable of reacting with the UV absorbent. Specifically, the UV absorbent may include hydroxyphenyltriazine based UV absorbents such as Tinuvin 400, Tinuvin 405, Tinuvin 460, and Tinuvin 479; hydroxyphenyl benzotriazol based UV absorbents such as Tinuvin 99, Tinuvin 99-2, Tinuvin 171, Tinuvin 328, Tinuvin 384-2, Tinuvin 900, Tinuvin 928, Tinuvin 1130, Tinuvin 5050, Tinuvin 5060, Tinuvin 5151, and Tinuvin P; benzophenone based UV absorbents such as Chimassorb 81 and Chimassorb 90, without being limited thereto. Specifically, the alkoxysilane compound may include trialkoxysilane having an isocyanate group. More specifically, the trialkoxysilane may contain an isocyanate group-containing C₁ to C₁₀ alkyl group and C₁ to C₁₀ alkoxy group. For example, the trialkoxysilane may be 3-(triethoxysilyl)propylisocyanate. Reaction between the UV absorbent and trialkoxysilane may be performed in a solvent at about 20° C. to about 80° C. for about 1 hour to about 12 hours. The solvent may be an organic solvent such as tetrahydrofuran. In reaction of the UV absorbent with trialkoxysilane, a catalyst may be used in order to improve reaction yield and may include a tin-based catalyst such as dibutyltin dilaurate. In another embodiment, the second silicon monomer may be obtained from commercially available products. For example, the second silicon monomer may include 2-hydroxy-4-(3-triethoxysilylpropoxy)diphenylketone, without being limited thereto.

Hydrolysis and condensation of the monomer mixture may be performed by a typical method for preparation of a siloxane resin. Hydrolysis may include reacting the first silicon monomer only or a mixture of the first silicon monomer and the second silicon monomer in a mixture of water and at least one of an acid and a base. Specifically, the acid may be a strong acid such as HCl and HNO₃ and the base may be a strong base such as NaOH and KOH. Hydrolysis may be performed at about 20° C. to about 100° C. for about 10 minutes to about 7 hours. Under these conditions, hydrolysis efficiency of the silicon monomers can be improved. Condensation may be performed at about 20° C. to about 100° C. for about 10 minutes to about 12 hours under the same conditions as hydrolysis. Under these conditions, hydrolysis efficiency of the silicon monomers can be improved. A platinum catalyst may be further used in order to improve efficiency in hydrolysis and condensation. The platinum catalyst may include a vinylalkylsilane platinum complex including a Karstedt catalyst, platinum black, chloroplatinic acid, a chloroplatinic acid-olefin complex, a chloroplatinic acid-alcohol complex, or a mixture thereof.

Next, a method of preparing the siloxane resin comprising the compound represented by Chemical Formula 2 will be described in detail.

The siloxane resin comprising the compound represented by Chemical Formula 2 may be prepared through hydrolysis and condensation of a monomer mixture including a first silicon monomer, a second silicon monomer, and a third silicon monomer. In the monomer mixture, the first silicon monomer may be present in an amount of about 40 mol % to about 99 mol %, specifically about 80 mol % to about 98 mol %. In the monomer mixture, the second silicon monomer may be present in an amount of about 0.1 mol % to about 20 mol %, specifically about 0.1 mol % to about 10 mol %, more specifically about 1 mol % to about 10 mol %. In the monomer mixture, the third silicon monomer may be present in an amount of about 0.1 mol % to about 40 mol %, specifically about 0.5 mol % to about 10 mol %, more specifically about 1 mol % to about 10 mol %. Within these ranges, the first to third silicon monomers can improve hardness, flexibility and light resistant reliability of the window film.

The first silicon monomer may include a silane compound represented by Chemical Formula 4, the second silicon monomer may include a silane compound represented by Chemical Formula 5, and the third silicon monomer may include a silane compound represented by Chemical Formula 6. These may be used alone or in combination thereof.

(wherein Chemical Formula 6, R³ and R⁴ are the same as defined in Chemical Formula 2, and R¹¹ and R¹² are each independently a halogen, a hydroxyl group or a C₁ to C₁₀ alkoxy group). Specifically, the third silicon monomer may include at least one selected from among 2-(3,4-epoxycyclohexyl)ethylmethyldiethoxysilane, dimethyldimethoxysilane, (3-glycidoxypropyl)methyldiethoxysilane, and ethylmethyldiethoxysilane, without being limited thereto.

Next, a flexible window film according to one embodiment will be described with reference to FIG. 1. FIG. 1 is a cross-sectional view of a flexible window film according to one embodiment of the invention.

Referring to FIG. 1, a flexible window film (100) according to one embodiment of the invention may include a base layer (110) and a coating layer (120), in which the coating layer (120) may be formed of the composition for window films according to the embodiment of the present invention.

The flexible window film (100) may have a curling of about 1.0 mm or less. Within this range, the flexible window film suffers from less curling and can be used as a window film for flexible displays.

The flexible window film (100) may have a pencil hardness of about 7H or higher, a radius of curvature of about 5.0 mm or less, and a ΔY.I. of about 5.0 or less. Within this range, the flexible window film exhibits good properties in terms of hardness, flexibility and light resistant reliability and can be used as a window film for flexible displays. Specifically, the flexible window film (100) may have a pencil hardness of about 7H to 9H, a radius of curvature of about 0.1 mm to about 5.0 mm, and a ΔY.I. of about 0.1 to about 5.0.

The base layer (110) can improve mechanical strength of the flexible window film (100) by supporting the coating layer (120) of the flexible window film (100). The base layer (110) may be attached to a display part, a touchscreen panel or a polarizing plate via an adhesive layer or the like.

The base layer (110) may be formed of an optically transparent flexible resin. For example, the resin may include polyester resins including polyethylene terephthalate, polyethylene naphthalate, polybutylene terephthalate, polybutylene naphthalate, and the like, polycarbonate resins, polyimide resins, polystyrene resins, poly(meth)acrylate resins including polymethylmethacrylate, and the like. These resins may be used alone or as a mixture thereof.

The base layer (110) may have a thickness of about 10 μm to about 200 μm, specifically about 20 μm to about 150 μm, more specifically about 50 μm to about 100 μm. Within this range, the base layer can be used in the flexible window film.

The coating layer (120) may be formed on the base layer (110) to protect the base layer (110), the display part, the touchscreen panel or the polarizing plate, and has high flexibility and high hardness to be used for a flexible display.

The coating layer (120) may have a thickness of about 5 μm to about 100 μm, specifically about 10 μm to about 80 μm. Within this range, the coating layer can be used in the flexible window film.

Although not shown in FIG. 1, functional surface layers such as an anti-reflection layer, an anti-glare layer, and a hard coating layer may be further formed on the other surface of the coating layer (120) to provide additional functions. In addition, although not shown in FIG. 1, the coating layer (120) may be further formed on the other surface of the base layer (110).

The flexible window film (100) is optically transparent and may be used in a transparent display. Specifically, the flexible window film (100) may have a transmittance of about 88% or more, specifically about 88% to about 100%, in the visible range, specifically in a wavelength range of 400 nm to 800 nm. Within this range, the flexible window film can be used as a window film for flexible displays.

The flexible window film (100) may have a thickness of about 50 μm to about 300 μm. Within this range, the flexible window film can be used as a window film for flexible displays.

The flexible window film (100) may be formed by coating and curing the composition for window films according to the embodiments on the base layer (110).

A method of coating the composition for window films onto the base layer (110) is not particularly limited. For example, the composition for window films may be coated onto the base layer by bar coating, spin coating, dip coating, roll coating, flow coating, or die coating. The composition for window films may be coated to a thickness of about 5 μm to about 100 μm on the base layer (110). Within this thickness range, a desired coating layer can be secured while providing good hardness, flexibility and reliability.

Curing is performed to form the coating layer by curing the composition for window films, and may include at least one of photocuring and heat curing. Photocuring may include irradiating the coated composition at a dose of about 10 mJ/cm² to about 1,000 mJ/cm² at a wavelength of 400 nm or less. Heat curing may be performed at a temperature of about 40° C. to about 200° C. for about 1 hour to about 30 hours. Under these conditions, the composition for window films can be sufficiently cured. For example, heat curing may be performed after photocuring in order to achieve higher hardness of the coating layer.

Before curing the composition for window films coated onto the base layer (110), the method may further include drying the composition. When curing is performed after drying, it is possible to prevent increase in surface roughness of the coating layer due to photocuring or heat curing for a long period of time. Drying may be performed at about 40° C. to about 200° C. for about 1 minute to about 30 hours, without being limited thereto.

Next, a flexible window film according to another embodiment will be described with reference to FIG. 2. FIG. 2 is a cross-sectional view of a flexible window film according to another embodiment of the invention.

Referring to FIG. 2, a flexible window film (200) according to another embodiment of the invention may include a base layer (110), a coating layer (120) formed on one surface of the base layer (110), and an adhesive layer (130) formed on the other surface of the base layer (110), in which the coating layer (120) may be formed of the composition for window films according to the embodiment of the present invention.

The flexible window film (200) may have a curling of about 1.0 mm or less, a pencil hardness of about 7H or higher, a radius of curvature of about 5.0 mm or less, and a ΔY.I. of about 5.0 or less. Within this range, the flexible window film exhibits good properties in terms of hardness, flexibility and light resistant reliability and can be used as a window film for flexible displays.

The adhesive layer (130) formed on the other surface of the base layer (110) can facilitate adhesion between the flexible window film and a touchscreen panel, a polarizing plate or a display part. The flexible window film according to this embodiment is substantially the same as the flexible window film according to the above embodiment excluding the adhesive layer. Thus, the following description will be given of the adhesive layer alone.

The adhesive layer (130) attaches a polarizing plate, a touchscreen panel, or a display part to the flexible window film (200) to be disposed under the flexible window film (200), and may be formed of an adhesive composition for the adhesive layer. Specifically, the adhesive layer (130) may be formed of an adhesive composition comprising an adhesive resin such as a (meth)acrylic resin, a urethane resin, a silicone resin, and an epoxy resin, a curing agent, a photoinitiator, and a silane coupling agent.

The (meth)acrylic resin is a (meth)acrylic copolymer having an alkyl group, a hydroxyl group, an aromatic group, a carboxylic acid group, an alicyclic group, a hetero-alicyclic group, and the like, and may include a typical (meth)acrylic copolymer. Specifically, the (meth)acrylic resin may be formed of a monomer mixture including at least one of a (meth)acrylic monomer containing a C₁ to C₁₀ unsubstituted alkyl group, a (meth)acrylic monomer containing a C₁ to C₁₀ alkyl group having at least one hydroxyl group, a (meth)acrylic monomer containing a C₆ to C₂₀ aromatic group, a (meth)acrylic monomer containing a carboxylic acid group, a (meth)acrylic monomer containing a C₃ to C₂₀ alicyclic group, and a (meth)acrylic monomer containing a C₃ to C₁₀ hetero-alicyclic group having at least one of nitrogen (N), oxygen (O), and sulfur (S).

The curing agent is a polyfunctional (meth)acrylate and may include a bifunctional (meth)acrylate such as hexanediol diacrylate; a trifunctional (meth)acrylate such as trimethylolpropane tri(meth)acrylate; a tetra-functional (meth)acrylate such as pentaerythritol tetra(meth)acrylate; a penta-functional (meth)acrylate such as dipentaerythritol penta(meth)acrylate; and a hexa-functional (meth)acrylate such as dipentaerythritol hexa(meth)acrylate, without being limited thereto.

The photoinitiator is a typical photoinitiator and may include the photo-radical initiator described above.

The silane coupling agent may include an epoxy group-containing silane coupling agent such as 3-glycidoxypropyltrimethoxysialne.

The adhesive composition may include 100 parts by weight of the (meth)acrylic resin, about 0.1 parts by weight to about 30 parts by weight of the curing agent, about 0.1 parts by weight to about 10 parts by weight of the photoinitiator, and about 0.1 parts by weight to about 20 parts by weight of the silane coupling agent. With this composition, the adhesive layer formed of the adhesive composition allows the flexible window film to be sufficiently attached to the display part, the touchscreen panel, or the polarizing plate.

The adhesive layer (130) may have a thickness of about 10 μm to about 100 μm. Within this range, the adhesive layer can sufficiently attach the flexible window film to an optical device such as a polarizing plate.

Next, a flexible display according to one embodiment will be described with reference to FIG. 3 and FIG. 4. FIG. 3 is a cross-sectional view of a flexible display according to one embodiment of the present invention and FIG. 4 is a cross-sectional view of one embodiment of a display part shown in FIG. 3.

Referring to FIG. 3, a flexible display (300) according to one embodiment of the invention includes a display part (350 a), an adhesive layer (360), a polarizing plate (370), a touchscreen panel (380), and a flexible window film (390), which may include the flexible window film according to the embodiments of the invention.

The display part (350 a) serves to drive the flexible display (300) and may include a substrate and an optical device formed on the substrate and including an OLED, an LED or an LCD device. FIG. 4 is a cross-sectional view of one embodiment of the display part shown in FIG. 3. Referring to FIG. 4, the display part (350 a) includes a lower substrate (310), a thin film transistor (316), an organic light emitting diode (315), a flattening layer (314), a protective layer (318), and an insulating layer (317).

The lower substrate (310) supports the display part (350 a), and the thin film transistor (316) and the organic light emitting diode (315) may be formed on the lower substrate (310). The lower substrate (310) may be formed with a flexible printed circuit board (FPCB) for driving the touchscreen panel (380). The flexible printed circuit board may further include a timing controller, a power source, and the like in order to drive an array of organic light emitting diodes.

The lower substrate (310) may include a substrate formed of a flexible resin. Specifically, the lower substrate (310) may include a flexible substrate such as a silicone substrate, a polyimide substrate, a polycarbonate substrate, and a polyacrylate substrate, without being limited thereto.

In a display area of the lower substrate (310), plural pixel domains are defined by plural driving wires (not shown) and plural sensor wires (not shown) intersecting each other and each of the pixel domains may be formed with an array of organic light emitting diodes, each of which includes the thin film transistor (316) and the organic light emitting diode (315) connected to the thin film transistor (316). In a non-display area of the lower substrate, a gate driver applying electric signals to the driving wires may be formed in the form of a gate-in panel. The gate-in panel circuit may be formed at one or both sides of the display area.

The thin film transistor (316) controls electric current flowing through a semiconductor by application of an electric field perpendicular to the electric current and may be formed on the lower substrate (310). The thin film transistor (316) may include a gate electrode (310 a), a gate insulation layer (311), a semiconductor layer (312), a source electrode (313 a), and a drain electrode (313 b). The thin film transistor (316) may be an oxide thin film transistor which uses an oxide such as indium gallium zinc oxide (IGZO), ZnO, or TiO as the semiconductor layer, an organic thin film transistor which uses an organic material as the semiconductor layer (312), an amorphous silicon thin film transistor which uses amorphous silicon as the semiconductor layer, or a polycrystalline silicon thin film transistor which uses polycrystalline silicon as the semiconductor layer.

The flattening layer (314) covers the thin film transistor (316) and a circuit section (310 b) to flatten upper surfaces of the thin film transistor (316) and the circuit section (310 b) such that the organic light emitting diode (315) can be formed thereon. The flattening layer (314) may be formed of a spin-on-glass (SOG) film, a polyimide polymer, or a polyacrylic polymer, without being limited thereto.

The organic light emitting diode (315) realizes a display through self-emission, and may include a first electrode (315 a), an organic light-emitting layer (315 b), and a second electrode (315 c), which are stacked in the stated order. Adjacent organic light emitting diodes may be isolated from each other by the insulating layer (317). The organic light emitting diode (315) may have a bottom emission type structure wherein light generated from the organic light-emitting layer (315 b) is emitted through the lower substrate, or a top-emission type structure wherein light from the organic light-emitting layer (315 b) is emitted through an upper substrate.

The protective layer (318) covers the organic light emitting diodes (315) to protect the organic light emitting diodes (315). The protective layer (318) may be formed of an inorganic material such as SiOx, SiNx, SiC, SiON, SiONC, and amorphous carbon (a-C), or an organic material such as (meth)acrylates, epoxy polymers, imide polymers, and the like. Specifically, the protective layer (318) may include an encapsulation layer in which an inorganic material layer and an organic material layer are sequentially stacked once or plural times.

Referring again to FIG. 3, the adhesive layer (360) serves to attach the display part (350 a) to the polarizing plate (370), and may be formed of an adhesive composition including a (meth)acrylate resin, a curing agent, an initiator, and a silane coupling agent.

The polarizing plate (370) can realize polarization of internal light or prevent reflection of external light to realize a display, or can increase contrast of the display. The polarizing plate may be composed of a polarizer alone. Alternatively, the polarizing plate may include a polarizer and a protective film formed on one or both surfaces of the polarizer. Alternatively, the polarizing plate may include a polarizer and a protective coating layer formed on one or both surfaces of the polarizer. As the polarizer, the protective film and the protective coating layer, a typical polarizer, a typical protective film and a typical protective coating layer known in the art may be used.

The touchscreen panel (380) generates electrical signals through detection of variation in capacitance when a human body or a conductor such as a stylus touches the touchscreen panel, and the display part (350 a) may be driven by such electrical signals. The touchscreen panel (380) is formed by patterning a flexible conductor, and may include first sensor electrodes and second sensor electrodes each formed between the first sensor electrodes and intersecting the first sensor electrodes. The touchscreen panel (380) may include a conductive material such as metal nanowires, conductive polymers, and carbon nanotubes, without being limited thereto.

The flexible window film (390) may be disposed as an outermost layer of the flexible display (300) to protect the flexible display.

Although not shown in FIG. 3, adhesive layers may be further formed between the polarizing plate (370) and the touchscreen panel (380) and/or between the touchscreen panel (380) and the flexible window film (390) to reinforce coupling between the polarizing plate, the touchscreen panel, and the flexible window film. The adhesive layers may be formed of an adhesive composition including a (meth)acrylate resin, a curing agent, an initiator, and a silane coupling agent. Although not shown in FIG. 3, a polarizing plate may be disposed under the display part (350 a) to realize polarization of internal light.

Next, a flexible display according to another embodiment of the present invention will be described with reference to FIG. 5. FIG. 5 is a cross-sectional view of a flexible display according to another embodiment of the present invention.

Referring to FIG. 5, a flexible display (400) according to another embodiment of the invention includes a display part (350 a), a touchscreen panel (380), a polarizing plate (370), and a flexible window film (390), which may include the flexible window film according to the embodiments of the invention. The flexible display according to this embodiment is substantially the same as the flexible display according to the above embodiment except that the touchscreen panel (380) is disposed under the polarizing plate (370) instead of being directly formed on the flexible window film (390). In addition, the touchscreen panel (380) may be formed together with the display part (350 a). In this case, since the touchscreen panel (380) is formed together with the display part (350 a) on the display part (350 a), the flexible display according to this embodiment is thinner and brighter than the flexible display according to the above embodiment, thereby providing better visibility. In addition, the touchscreen panel (380) may be formed by deposition, without being limited thereto. Although not shown in FIG. 5, adhesive layers may be further formed between the display part (350 a) and the touchscreen panel (380), between the touchscreen panel (380) and the polarizing plate (370), and/or between the polarizing plate (370) and the flexible window film (390) to reinforce mechanical strength of the display. The adhesive layers may be formed of an adhesive composition including a (meth)acrylate resin, a curing agent, an initiator, and a silane coupling agent. Although not shown in FIG. 5, a polarizing plate may be disposed under the display part (350 a) to provide a good display image through polarization of internal light.

Next, a flexible display according to a further embodiment of the present invention will be described with reference to FIG. 6. FIG. 6 is a cross-sectional view of a flexible display according to a further embodiment of the present invention. Referring to FIG. 6, a flexible display (500) according to a further embodiment of the invention includes a display part (350 b), an adhesive layer (360), and a flexible window film (390), which may include the flexible window film according to the embodiments of the invention. The flexible display according to this embodiment is substantially the same as the flexible display according to the one embodiment except that the flexible display can be driven by the display part (350 b) alone and the polarizing plate and the touchscreen panel are omitted.

The display part (350 b) may include a substrate and an optical device formed on the substrate and including an OLED, an LED or an LCD device. The display part (350 b) may further include a touchscreen panel therein.

Although the flexible window films according to the embodiments of the invention are described as being applied to a flexible display, it should be understood that the flexible window films according to the embodiments of the invention may also be applied to a non-flexible display.

Hereinafter, the present invention will be described in more detail with reference to some examples. It should be understood that these examples are provided for illustration only and are not to be construed in any way as limiting the present invention.

Example 1

50 g of a monomer mixture comprising 95 mol % of 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane and 5 mol % of 2-hydroxy-4-(3-triethoxysilylpropoxy)diphenylketone was placed in a 200 ml 2-neck flask. To the monomer mixture, 2 mol % of KOH and 1 mol % of water were added, followed by stirring at 65° C. for 4 hours. A siloxane resin was prepared by removing remaining water and alcohol using a vacuum distillation device, and methylethylketone was added thereto to obtain 90 wt % of the siloxane resin in terms of solid content. The siloxane resin had a weight average molecular weight of 6,200 as measured by gel permeation chromatography.

A composition for window films was prepared by mixing 100 parts by weight of the prepared siloxane resin, 10 parts by weight of a crosslinking agent CY-179 (Araldite), and 5 parts by weight of an initiator CPI-100P (SAN-APRO). The prepared composition was coated onto a polyethylene terephthalate film (TA043, Toyobo, thickness: 80 μm), followed by drying at 100° C. for 5 minutes, irradiation with UV light at 1,000 mJ/cm², and heating at 80° C. for 4 hours, thereby preparing a window film having a 50 μm thick coating layer.

Example 2

A window film was prepared in the same manner as in Example 1 except that 10 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.) was used instead of 10 parts by weight of the crosslinking agent CY-179.

Example 3

A window film was prepared in the same manner as in Example 1 except that 10 parts by weight of OXT-221 (3-ethyl-3[[(3-ethyloxetane-3-yl)methoxy]methyl]oxetane, Toagosei) was used instead of 10 parts by weight of the crosslinking agent CY-179.

Example 4

A window film was prepared in the same manner as in Example 1 except that 20 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.) was used instead of 10 parts by weight of the crosslinking agent CY-179.

Example 5

A window film was prepared in the same manner as in Example 1 except that 30 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.) was used instead of 10 parts by weight of the crosslinking agent CY-179.

Example 6

(1) Preparation of Second Silicon Monomer (Tinuvin 400-Derived Triethoxysilane)

50.0 g of Tinuvin-400 (BASF) and 150 ml of toluene were mixed in a 1 L round bottom flask. After washing the mixture three times with 150 ml of distilled water using a separatory funnel, an organic layer was collected, followed by vacuum enrichment and drying. The obtained concentrate was dissolved in 85 ml of tetrahydrofuran, and 17.06 g of 3-(triethoxysilyl)propylisocyanate and 1.0 g of a 5% tetrahydrofuran solution in which dibutyltin dilaurate was dissolved were further added thereto. Reaction was performed by refluxing at 65° C. for 3 hours, followed by cooling to room temperature, and completion of the reaction was confirmed through NMR. The obtained solution was completely dried through vacuum enrichment, thereby obtaining Tinuvin 400-derived triethoxysilane, which is a solid phase mixture of a second silicon monomer represented by Chemical Chemical Formula ii and a second silicon monomer represented by Chemical Chemical Formula iii.

(2) Preparation of Window Film

50 g of a monomer mixture comprising 95 mol % of 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane (Sigma-Aldrich) and 5 mol % of the prepared Tinuvin 400-derived triethoxysilane was placed in a 200 ml 2-neck flask. To the monomer mixture, 2 mol % of KOH and 1 mol % of water were added, followed by stirring at 65° C. for 4 hours. A siloxane resin was prepared by removing remaining water and alcohol using a vacuum distillation device, and methylethylketone was added thereto to obtain 90 wt % of the siloxane resin in terms of solid content. The siloxane resin had a weight average molecular weight of 6,200 as measured by gel permeation chromatography.

A composition for window films was prepared by mixing 100 parts by weight of the prepared siloxane resin, 20 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.), and 5 parts by weight of an initiator CPI-100P (SAN-APRO). A window film was prepared using the prepared siloxane resin in the same manner as in Example 1.

Example 7

A siloxane resin was prepared in the same manner as in Example 1 except that a monomer mixture was prepared by mixing 98 mol % of 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, 1 mol % of 2-hydroxy-4-(3-triethoxysilylpropoxy)diphenylketone, and 1 mol % of dimethyldimethoxysilane. A composition for window films was prepared by mixing 100 parts by weight of the prepared siloxane resin, 20 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.), and 5 parts by weight of an initiator CPI-100P (SAN-APRO). A window film was prepared using the prepared siloxane resin in the same manner as in Example 1.

Example 8

A siloxane resin was prepared in the same manner as in Example 1 except that a monomer mixture was prepared by mixing 98 mol % of 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, 1 mol % of 2-hydroxy-4-(3-triethoxysilylpropoxy)diphenylketone, and 1 mol % of 2-(3,4-epoxycyclohexyl)ethylmethyldiethoxysilane. A composition for window films was prepared by mixing 100 parts by weight of the prepared siloxane resin, 20 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.), and 5 parts by weight of an initiator CPI-100P (SAN-APRO). A window film was prepared using the prepared siloxane resin in the same manner as in Example 1.

Example 9

Tinuvin 400-derived triethoxysilane was prepared in the same manner as in Example 6. A siloxane resin was prepared in the same manner as in Example 1 except that a monomer mixture was prepared by mixing 98 mol % of 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, 1 mol % of Tinuvin 400-derived triethoxysilane, and 1 mol % of dimethyldimethoxysilane. A composition for window films was prepared by mixing 100 parts by weight of the prepared siloxane resin, a mixture of 10 parts by weight of CY-179 (Araldite) and 10 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.) as a crosslinking agent, and 5 parts by weight of an initiator CPI-100P (SAN-APRO). A window film was prepared using the prepared siloxane resin in the same manner as in Example 1.

Example 10

Tinuvin 400-derived triethoxysilane was prepared in the same manner as in Example 6. A siloxane resin was prepared in the same manner as in Example 1 except that a monomer mixture was prepared by mixing 98 mol % of 2-(3,4-epoxycyclohexyl)ethyltriethoxysilane, 1 mol % of Tinuvin 400-derived triethoxysilane, and 1 mol % of 2-(3,4-epoxycyclohexyl)ethylmethyldiethoxysilane. A composition for window films was prepared by mixing 100 parts by weight of the prepared siloxane resin, a mixture of 10 parts by weight of bis(3,4-epoxycyclohexylmethyl)adipate (JIANGSU TETRA NEW MATERIAL TECHNOLOGY Co.) and 10 parts by weight of OXT-221 (Toagosei) as a crosslinking agent, and 5 parts by weight of an initiator CPI-100P (SAN-APRO). A window film was prepared using the prepared siloxane resin in the same manner as in Example 1.

Example 11

400 g of a monomer mixture comprising 95 mol % of 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane (KBM-303, Shin-Etsu Chemicals Co., Ltd.) and 5 mol % of (3-glycidoxypropyl)trimethoxysilane (KBM-403, Shin-Etsu Chemicals Co., Ltd.) was placed in a 1 L 3-neck flask. To the monomer mixture, 0.1 mol % of KOH based on the amount of the monomer mixture and 1 equivalent weight of water based on the total amount of the silicon monomers were added, followed by stirring at 65° C. for 8 hours and washing with toluene. Then, a siloxane resin represented by (EcSiO_(3/2))_(0.95)(GpSiO_(3/2))_(0.05) (weight average molecular weight: 5,500 as measured by GPC) was prepared through concentration of the resulting material. A window film was prepared using the prepared siloxane resin in the same manner as in Example 1.

Comparative Examples 1 to 6

Window films were prepared in the same manner as in Example 1 except that the kind and mole ratio of silicon monomers in preparation of the siloxane resin and the kind and content of the crosslinking agent were changed, as listed in Table 2.

Details of the compositions for window films prepared in Examples and Comparative Examples are shown in Tables 1 and 2. The window films prepared in Examples and Comparative Examples were evaluated as to Properties (1) to (4) and evaluation results are shown in Table 1 and 2.

1. Curling: Referring to FIG. 7, a window film (1) including an 80 μm thick base layer and a 50 μm thick coating layer was cut to a size of length×width (10 cm×10 cm) and placed on a floor surface (2) such that the base layer contacted the floor surface (2). Then, the window film was left at 25° C. and at 50% relative humidity. Thereafter, a maximum height (H) from the floor surface (2) to an edge of the window film (1) was measured and averaged.

2. Pencil hardness: Pencil hardness was measured on a coating layer of a window film using a pencil hardness tester (Heidon) in accordance with JIS K5400. Pencil hardness was measured using pencils of 6B to 9H (Mitsubishi Co., Ltd.) under conditions of a pencil load of 1 kg on the coating layer, a scratch angle of 45°, and a scratch speed of 60 mm/m in. When the coating layer had one or more scratches after being tested 5 times using a certain pencil, pencil hardness was measured again using another pencil having one-level lower pencil hardness than the previous pencil. A pencil hardness value allowing no scratch to be observed all five times on the coating layer was taken as pencil hardness of the coating layer.

3. Radius of curvature: A window film (length×width×thickness, 3 cm×15 cm×130 μm, base layer thickness: 80 μm, coating layer thickness: 50 μm) was wound around a jig for measuring a radius of curvature (CFT-200R, COVOTECH Co., Ltd.), kept wound for 5 seconds or more, unwound, and then observed with the naked eye to determine whether the window film had cracks. Here, a radius of curvature in a compressive direction was measured by winding the window film around the jig such that the coating layer of the window film contacted the jig, and a radius of curvature in a tensile direction was measured by winding the window film around the jig such that the base layer of the window film contacted the jig. The radius of curvature was determined as a minimum radius of a jig causing no cracks on the window film, as measured in the compression direction while gradually decreasing the diameters of jigs from a jig having the maximum diameter.

4. Light resistant reliability: A yellow index (Y1) was measured on a window film under a D65 light source at 2° (angle between the window film and the light source) using a colorimeter (CM3600D, Konica Minolta). Then, a yellow index (Y2) was measured on the window film by the same method after irradiating the window film at a peak wavelength of 306 nm for 72 hours using a light resistance tester (CT-UVT, Core Technology Inc.). Light resistant reliability was determined based on a difference in yellow index (Y2−Y1, ΔY.I.) between before irradiation and after irradiation.

TABLE 1 Example 1 2 3 4 5 6 7 8 9 10 11 Silicon 2-(3,4- 95 95 95 95 95 95 98 98 98 98 — monomer epoxycyclohexyl)ethyl (mol %) triethoxysilane 2-hydroxy-4-(3- 5 5 5 5 5 — 1 1 — — — triethoxysilylpropoxy)diphenylketone Tinuvin 400- — — — — — 5 — — 1 1 — derived triethoxysilane Dimethyldimethoxysilane — — — — — — 1 — 1 — — 2-(3,4- — — — — — — — 1 — 1 — epoxycyclohexyl)ethyl methyldiethoxysilane 2-(3,4- — — — — — — — — — — 95 epoxycyclohexyl)ethyl trimethoxysilane (3- — — — — — — — — — — 5 glycidoxypropyl)trimethoxysilane Crosslinking CY-179 10 — — — — — — — 10 — 10 agent bis[(3,4- — 10 — 20 30 20 20 20 10 10 — (parts by epoxycyclohexyl)methyl]adipate weight) OXT-221 — — 10 — — — — — — 10 — Initiator (parts by weight) 5 5 5 5 5 5 5 5 5 5 5 Curling (mm) 0.9 0.8 1.0 0.6 0.3 0.6 0.5 0.4 0.8 0.9 0.3 Pencil hardness 7H 9H 7H 8H 7H 7H 8H 8H 7H 7H 8H Radius of curvature (mm) 3.7 3.5 3.8 3.3 3.1 3.6 2.8 3.0 3.4 3.5 2.9 Light resistant reliability (ΔY.I.) 2.1 2.1 2.0 1.9 2.0 2.2 1.9 2.0 2.2 2.1 1.8

TABLE 2 Comparative Example 1 2 3 4 5 6 Silicon 2-(3,4-epoxycyclohexyl)ethyl 95 95 98 98 95 95 monomer triethoxysilane (mol %) 2-hydroxy-4-(3- triethoxysilylpropoxy)diphenylketone 5 5 1 1 5 — Tinuvin 400-derived triethoxysilane — — — — — 5 Dimethyldimethoxysilane — — 1 — — — 2-(3,4- — — — 1 — — epoxycyclohexyl)ethylmethyldiethoxysilane Crosslinking CY-179 — — — — — — agent bis[(3,4-epoxycyclohexyl)methyl]adipate 5 35 5 35 — — (parts by OXT-221 — — — — — — weight) Initiator (parts by weight) 5 5 5 5 5 5 Curling (mm) 23 0 17 0 37 34 Pencil hardness 9H 2H 8H H 6H 7H Radius of curvature (mm) 5.6 3.6 5.7 3.5 6.4 6.0 Light resistance (ΔY.I.) 2.4 2.1 2.3 2.2 1.8 1.6

As shown in Table 1, the flexible window films of Examples had a small curl of 1 mm or less of curling, a pencil hardness of 7H or more meaning high hardness, a radius of curvature of 5.0 mm or less of good flexibility, and good light resistant reliability to be used as a window film for flexible displays.

As shown in Table 2, the flexible window films of Comparative Examples 1 to 4, in which the content of the crosslinking agent was not within the range of the present invention, had a high curl or exhibited poor properties in terms of at least one of pencil hardness, radius of curvature and light resistant reliability. The flexible window films of Comparative Examples 5 and 6, which did not include the crosslinking agent, exhibited poorer properties in terms of curling and radius of curvature.

It should be understood that various modifications, changes, alterations, and equivalent embodiments can be made by those skilled in the art without departing from the spirit and scope of the invention. 

The invention claimed is:
 1. A composition for window films, comprising: a siloxane resin represented by Chemical Formula 1 or a siloxane resin represented by Chemical Formula 2 or a mixture thereof, a crosslinking agent, and an initiator, wherein the crosslinking agent is present in an amount of about 10 parts by weight to about 30 parts by weight relative to 100 parts by weight of the siloxane resin or the mixture thereof: (R¹SiO_(3/2))_(x)(R²SiO_(3/2))_(y)  <Chemical Formula 1> (where, in Chemical Formula 1, R¹ is a crosslinkable functional group; R² is a UV absorption functional group or a UV absorption functional group-containing group; and 0<x<1, 0<y<1, and x+y=1), (R¹SiO_(3/2))_(x)(R³R⁴SiO_(2/2))_(z)(R²SiO_(3/2))_(y)  <Chemical Formula 2> (where, in Chemical Formula 2, R¹ is a crosslinkable functional group; R² is a UV absorption functional group or a UV absorption functional group-containing group; R³ and R⁴ are each independently hydrogen, a crosslinkable functional group, an unsubstituted or substituted C₁ to C₂₀ alkyl group, or an unsubstituted or substituted C₅ to C₂₀ cycloalkyl group, at least one of R³ and R⁴ being an unsubstituted or substituted C₁ to C₂₀ alkyl group; and 0<x<1, 0<y<1, 0<z<1, and x+y+z=1), wherein the siloxane resin represented by Chemical Formula 1 is represented by one of Chemical Formulae 1-1 to 1-12: (EcSiO_(3/2))_(x)(RaSiO_(3/2))_(y),  <Chemical Formula 1-1> (ECSiO_(3/2))_(x)(RbSiO_(3/2))_(y)  <Chemical Formula 1-2> (EcSiO_(3/2))_(x)(RcSiO_(3/2))_(y)  <Chemical Formula 1-3> (EcSiO_(3/2))_(x)(RdSiO_(3/2))_(y)  <Chemical Formula 1-4> (GpSiO_(3/2))_(x)(RaSiO_(3/2))_(y)  <Chemical Formula 1-5> (GpSiO_(3/2))_(x)(RbSiO_(3/2))_(y)  <Chemical Formula 1-6> (GpSiO_(3/2))_(x)(RcSiO_(3/2))_(y)  <Chemical Formula 1-7> (GpSiO_(3/2))_(x)(RdSiO_(3/2))_(y)  <Chemical Formula 1-8> (OpSiO_(3/2))_(x)(RaSiO_(3/2))_(y)  <Chemical Formula 1-9> (OpSiO_(3/2))_(x)(RbSiO_(3/2))_(y)  <Chemical Formula 1-10> (OpSiO_(3/2))_(x)(RcSiO_(3/2))_(y)  <Chemical Formula 1-11> (OpSiO_(3/2))_(x)(RdSiO_(3/2))_(y)  <Chemical Formula 1-12> (where, in Chemical Formulae 1-1 to 1-12, Ec is a (3,4-epoxycyclohexyl)ethyl group, Gp is a 3-glycidoxy propyl group, Op is a 3-oxetanylpropyl group, 0<x<1, 0<y<1, and x+y=1, Ra is represented by Chemical Formula i), Rb is represented by Chemical Formula ii), Rc is represented by Chemical Formula iii), and Rd is represented by Chemical Formula iv),

(in Chemical Formulae i to iv, * is a linking site).
 2. The composition for window films according to claim 1, wherein the crosslinking agent comprises a cyclic aliphatic epoxy monomer.
 3. The composition for window films according to claim 2, wherein the cyclic aliphatic epoxy monomer comprises at least one selected from (3,4-epoxycyclohexyl)methyl-3′,4′-epoxyyclohexanecarboxylate, 3,4-epoxy-6-methylcyclohexylmethyl-3′,4′-epoxy-6′-methylyclohexanecarboxylate, bis(3,4-epoxycyclohexylmethyl)adipate, bis((3,4-epoxy-6-methylcyclohexyl)methyl)adipate, bis(3,4-epoxycyclohexylmethyl)malonate, bis(3,4-epoxycyclohexylmethyl)succinate, bis(3,4-epoxycyclohexylmethyl)glutarate, bis(3,4-epoxycyclohexylmethyl)pimelate, bis(3,4-epoxycyclohexylmethyl)azelate, and bis(3,4-epoxycyclohexylmethyl)sebacate.
 4. A flexible window film comprising a base layer and a coating layer formed on one surface of the base layer, wherein the flexible window film has a curling of about 1.0 mm or less and the coating layer is formed of the composition for window films according to claim
 1. 5. The flexible window film according to claim 4, further comprising: an adhesive layer formed on the other surface of the base layer.
 6. A flexible display comprising the flexible window film according to claim
 4. 7. The flexible display according to claim 6, wherein the flexible display comprises a display part, an adhesive layer formed on the display part, a polarizing plate formed on the adhesive layer, a touchscreen panel formed on the polarizing plate, and the flexible window film formed on the touchscreen panel.
 8. The flexible display according to claim 6, wherein the flexible display comprises a display part, a touchscreen panel formed on the display part, a polarizing plate formed on the touchscreen panel, and the flexible window film formed on the polarizing plate.
 9. The flexible display according to claim 6, wherein the flexible display comprises a display part, an adhesive layer formed on the display part, and the flexible window film formed on the adhesive layer.
 10. The flexible display according to claim 9, wherein the display part further comprises a polarizing plate disposed at an upper or lower side thereof.
 11. A composition for window films, comprising: a siloxane resin represented by Chemical Formula 1 or a siloxane resin represented by Chemical Formula 2 or a mixture thereof, a crosslinking agent, and an initiator, wherein the crosslinking agent is present in an amount of about 10 parts by weight to about 30 parts by weight relative to 100 parts by weight of the siloxane resin or the mixture thereof: (R¹SiO_(3/2))_(x)(R²SiO_(3/2))_(y)  <Chemical Formula 1> (where, in Chemical Formula 1, R¹ is a crosslinkable functional group; R² is a UV absorption functional group or a UV absorption functional group-containing group; and 0<x≤1, 0≤y<1, and x+y=1), R¹SiO_(3/2))_(x)(R³R⁴SiO_(2/2))_(z)(R²SiO_(3/2))_(y)  <Chemical Formula 2> (where, in Chemical Formula 2, R¹ is a crosslinkable functional group; R² is a UV absorption functional group or a UV absorption functional group-containing group; R³ and R⁴ are each independently hydrogen, a crosslinkable functional group, an unsubstituted or substituted C₁ to C₂₀ alkyl group, or an unsubstituted or substituted C₅ to C₂₀ cycloalkyl group, at least one of R³ and R⁴ being an unsubstituted or substituted C₁ to C₂₀ alkyl group; and 0<x<1, 0<y<1, 0<z<1, and x+y+z=1), wherein the composition for window films comprises a compound represented by Chemical Formula 1-13: (EcSiO_(3/2))_(x1)(GpSiO_(3/2))_(x2)  <Chemical Formula 1-13> (where, in Chemical Formula 1-13, Ec is a (3,4-epoxycyclohexyl)ethyl group, Gp is a 3-glycidoxy propyl group, and 0<x1<1, 0<x2<1, and x1+x2=1). 